Nitrogen-Doped Carbon Matrix to Optimize Cycling Stability of Lithium Ion Battery Anode from SiOx Materials

IF 3.1 4区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Xuan Bie, Yawei Dong, M. Xiong, Ben Wang, Zhongxue Chen, Qunchao Zhang, Yi Liu, Ronghua Huang
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引用次数: 0

Abstract

This study prepared silicon oxide anode materials with nitrogen-doped carbon matrices (SiOx/C–N) through silicon-containing polyester thermal carbonization. Melamine was introduced as a nitrogen source during the experiment. This nitrogen doping process resulted in a porous structure in the carbon matrices, a fact confirmed by scanning electron microscopy (SEM). Pyridinic and quaternary nitrogen, but mainly tertiary nitrogen, were generated, as shown via X-ray photoelectron spectroscopy (XPS). Electrochemical tests confirmed that, as anode materials for a lithium-ion battery, SiOx/C–N provided better cycle stability, improved rate capability, and lower Li+ diffusion resistance. The best performance showed an activated capacity at 493.5 mAh/g, preserved at 432.8 mAh/g after the 100th cycle, with 87.7% total Columbic efficiency. Those without nitrogen doping gave 1126.7 mAh/g, 249.0 mAh/g, and 22.1%, respectively. The most noteworthy point was that, after 100 cycles, anodes without nitrogen doping were pulverized into fine powders (SEM); meanwhile, in the case of anodes with nitrogen doping, powders of a larger size (0.5–1.0 µm) formed, with the accumulation of surrounding cavities. We suggest that the formation of more prominent powders may have resulted from the more substantial nitrogen-doped carbon matrices, which prevented the anode from further breaking down to a smaller size. The volume expansion stress decreased when the powders decreased to nanosize, which is why the nanosized silicon anode materials showed better cycling stability. When the anodes were cracked into powders with a determined diameter, the stress from volume expansion decreased to a level at which the powders could preserve their shape, and the breakage of the powders was stopped. Hence, the diameters of the final reserved powders are contingent on the strength of the matrix. As reported, nitrogen-doped carbon matrices are more robust than those not doped with nitrogen. Thus, in our research, anodes with nitrogen-doped carbon matrices presented more large-diameter powders, as SEM confirmed. Anodes with nitrogen doping will not be further broken at a larger diameter. At this point, the SEI film will not show continuous breakage and formation compared to the anode without doping. This was validated by the lower deposition content of the SEI-film-related elements (phosphorous and fluorine) in the cycled anodes with nitrogen doping. The anode without nitrogen doping presented higher content, meaning that the SEI films were broken many times during lithiation/delithiation (EDS mapping).
掺氮碳基质优化氧化硅材料锂离子电池负极的循环稳定性
本研究通过含硅聚酯热碳化法制备了具有掺氮碳基质(SiOx/C-N)的氧化硅阳极材料。实验过程中引入了三聚氰胺作为氮源。扫描电子显微镜(SEM)证实了这一事实。X 射线光电子能谱(XPS)显示,产生了吡啶氮和四氮,但主要是三氮。电化学测试证实,作为锂离子电池的负极材料,SiOx/C-N 具有更好的循环稳定性、更高的速率能力和更低的 Li+ 扩散阻力。最佳性能显示,活化容量为 493.5 mAh/g,第 100 次循环后仍保持在 432.8 mAh/g,总哥伦布效率为 87.7%。未掺氮的电池容量分别为 1126.7 毫安时/克、249.0 毫安时/克和 22.1%。最值得注意的一点是,在 100 个循环后,未掺氮的阳极被粉碎成细小的粉末(扫描电镜);而掺氮的阳极则形成了较大尺寸(0.5-1.0 µm)的粉末,周围的空穴也随之堆积。我们认为,形成更为突出的粉末可能是由于掺氮碳基质更为坚实,从而阻止了阳极进一步分解至更小的尺寸。当粉末减小到纳米尺寸时,体积膨胀应力减小,这就是为什么纳米硅阳极材料显示出更好的循环稳定性。当阳极裂解成直径确定的粉末时,体积膨胀应力降低到粉末可以保持形状的水平,粉末的破裂也随之停止。因此,最终保留的粉末直径取决于基体的强度。据报道,掺氮的碳基质比未掺氮的碳基质更坚固。因此,在我们的研究中,掺氮碳基质的阳极呈现出更多的大直径粉末,扫描电镜也证实了这一点。掺氮阳极在直径较大时不会进一步破碎。此时,与未掺氮的阳极相比,SEI 膜不会出现连续断裂和形成。在掺氮的循环阳极中,SEI 膜相关元素(磷和氟)的沉积含量较低,从而验证了这一点。而未掺氮的阳极中的含量更高,这意味着 SEI 膜在锂化/退锂过程中多次断裂(EDS 图谱)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Inorganics
Inorganics Chemistry-Inorganic Chemistry
CiteScore
2.80
自引率
10.30%
发文量
193
审稿时长
6 weeks
期刊介绍: Inorganics is an open access journal that covers all aspects of inorganic chemistry research. Topics include but are not limited to: synthesis and characterization of inorganic compounds, complexes and materials structure and bonding in inorganic molecular and solid state compounds spectroscopic, magnetic, physical and chemical properties of inorganic compounds chemical reactivity, physical properties and applications of inorganic compounds and materials mechanisms of inorganic reactions organometallic compounds inorganic cluster chemistry heterogenous and homogeneous catalytic reactions promoted by inorganic compounds thermodynamics and kinetics of significant new and known inorganic compounds supramolecular systems and coordination polymers bio-inorganic chemistry and applications of inorganic compounds in biological systems and medicine environmental and sustainable energy applications of inorganic compounds and materials MD
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